Helaina Inc., New York, NY, USA.
Nutrition Program, School of Biological and Population Health Sciences, College of Public Health and Human Sciences, and Department of Food Science and Technology, Oregon State University, Corvallis, OR, USA.
Food Chem Toxicol. 2024 Jul;189:114727. doi: 10.1016/j.fct.2024.114727. Epub 2024 May 10.
Published studies on the glycosylation, absorption, distribution, metabolism, excretion, and safety outcomes of orally ingested recombinant human lactoferrin (rhLF) were reviewed in the context of unanswered safety questions, including alloimmunization, allergenicity, and immunotoxicity potential of rhLF during repeated exposure. The primary objective was to summarize current safety data of rhLF produced in transgenic host expression systems. Overall, results from animal and human studies showed that rhLF was well tolerated and safe. Animal data showed no significant toxicity-related outcomes among any safety or tolerability endpoints. The no observed adverse effect levels (NOAEL) were at the highest level tested in both iron-desaturated and -saturated forms of rhLF. Although one study reported outcomes of rhLF on immune parameters, no animal studies directly assessed immunogenicity or immunotoxicity from a safety perspective. Data from human studies were primarily reported as adverse events (AE). They showed no or fewer rhLF-related AE compared to control and no evidence of toxicity, dose-limiting toxicities, or changes in iron status in various subpopulations. However, no human studies evaluated the immunomodulatory potential of rhLF as a measure of safety. Following this review, a roadmap outlining preclinical and clinical studies with relevant safety endpoints was developed to address the unanswered safety questions.
本文回顾了口服摄入重组人乳铁蛋白(rhLF)的糖基化、吸收、分布、代谢、排泄和安全性结果,以解答包括同种异体免疫、变应原性和重复暴露时 rhLF 的免疫毒性潜力等未解决的安全性问题。主要目的是总结转基因宿主表达系统生产的 rhLF 的现有安全性数据。总体而言,动物和人体研究结果表明 rhLF 具有良好的耐受性和安全性。动物数据显示,在任何安全性或耐受性终点中,均未出现与毒性相关的显著结果。rhLF 的铁去饱和和饱和形式的最高测试水平均达到了无观察到不良效应水平(NOAEL)。尽管有一项研究报告了 rhLF 对免疫参数的影响,但没有任何动物研究从安全性角度直接评估其免疫原性或免疫毒性。人体研究数据主要以不良事件(AE)报告。与对照组相比,rhLF 相关 AE 无或更少,且未发现毒性、剂量限制毒性或不同亚人群中铁状态的变化。然而,没有人体研究评估 rhLF 的免疫调节潜力作为安全性的衡量标准。在这项综述之后,制定了一份包含相关安全性终点的临床前和临床研究路线图,以解答未解决的安全性问题。